Identification of the CIPK-CBL family gene and functional characterization of CqCIPK14 gene under drought stress in quinoa

Background Calcineurin-like Protein (CBL) and CBL interacting protein kinase (CIPK) play a key role in plant signal transduction and response to various environmental stimuli. Quinoa, as an important plant with high nutritional value, can meet the basic nutritional needs of human Cash crop, is also susceptible to abiotic stress. However, CBL-CIPK in quinoa have not been reported. Results In this study, 16 CBL and 41 CIPK genes were identified in quinoa. CBL-CIPK gene shows different intron-exon gene structure and motif, they participate in different biological processes, and form a complex regulatory network between CBL-CIPK proteins. Many cis-regulatory element associated with ABA and drought have been found. The expression patterns of CBL-CIPK showed different expression patterns in various abiotic stresses and tissues. RT-qPCR showed that most members of these two gene families were involved in drought regulation of quinoa, in particular, the expression levels of CqCIPK11, CqCIPK15, CqCIPK37 and CqCBL13 increased significantly under drought stress. Conclusions The structures and functions of the CBL-CIPK family in quinoa were systematically explored. Many CBL-CIPK may play vital roles in the regulation of organ development, growth, and responses to abiotic stresses. This research has great significance for the functional characterisation of the quinoa CBL-CIPK family and our understanding of the CBL-CIPK family in higher plants. Supplementary Information The online version contains supplementary material available at 10.1186/s12864-022-08683-6.


Introduction
Under various abiotic stresses (such as drought, low temperature and high salt stress), plants will evolve a set of protective mechanisms to cope with the abiotic stresses and ensure the normal growth and development of plants [1]. Calcium, as the second messenger, plays an important role in plant stress signal transduction. It is widely involved in plant growth and development and regulates the response to environmental stress. Calcium can transform external signals into cytoplasmic information, to further drive a response to a particular stimulus [2]. There are four major calcium ion sensors in plants, including calmodulin (CAMs), calmodulin-like proteins (CMLs), calmodulin-dependent protein kinases (CDPKs) and calcineurin B-like proteins (CBLs), They perceive and modulate the response to calcium concentration of various stimuli [3]. Calcineurin B-like proteins (CBLs), as a unique calcium receptor in plants, can sense the changes of Ca 2+ in plants and combine with the CBL-interacting protein kinases (CIPKs) to form the CBL-CIPK complex, when stress occurs, the complex is phosphorylated with the corresponding target protein, and the signal is Open Access *Correspondence: weixh@gsau.edu.cn transmitted downstream to improve the stress response ability of the plant under stress [4].
As far as the CBL-CIPK protein complex is concerned, the CBL protein contains four typical helix-loop-helix motifs (EF-hands) for Ca 2+ binding, the EF-hand is a helix-loop-helix motif containing 12 + X• + Y• + Z•-Y•-X••-Z residues, where the letters represent the ligands involved in metal coordination and dots represent the intervening residues [5]. CIPKs is a family of small plantspecific serine/threonine (Ser/Thr) protein kinase, also known as SnRK3 protein family [6]. CIPKs usually contain a conserved N-terminal kinase domain and C-terminal regulatory domain, and the C-terminal regulatory domain contains a highly conserved NAF/FISL domain, which contains 24 amino acids consisting of highly conserved N, A and F (NAF) or F, I, S and L (FISL), its role is to interact with CBL and release itself from selfinhibition, thereby enabling the substrate to bind to the kinase domain, NAF/FISL is followed by a PPI motif, PPI motif contains about 37 amino acids, which can be combined with PP2C (protein phosphatase), an inhibitor of CIPK kinase activity [7]. The conserved N-terminus is a serine/threonine protein kinase catalytic domain. The N-terminal kinase domain has an ATP binding site and an activation segment. The activation segment contains a phosphorylated activation loop. Amino acid phosphorylation activates the kinase, and the N-terminus of CIPK is similar to the N-terminal kinase domain found in other plant protein kinases, containing a catalytic structure and an activation structure [8]. As target proteins of CBL, CIPKs together with CBLs form a Ca 2+ -mediated CBL-CIPK regulatory network.
Quinoa (Chenopodium quinoa Willd.) is an annual dicotyledonous herb, rich in protein, amino acids, minerals and other nutrients, so it enjoys the title of "super grain" [30]. Quinoa has excellent biological characteristics of cold-tolerance, drought-tolerance, salt-tolerance and barren-tolerance, so it is very suitable for planting in arid and semi-arid areas of northwest China. CBLs and CIPKs, as key components of plant perception and transmission of calcium signals, play a crucial role in plant responses to abiotic stresses [9,10]. However, the function of the CIPK-CBL gene in quinoa is largely unknown. In 2017, the completion of quinoa genome sequence [30] provided an opportunity to systematically study the quinoa CIPK-CBL gene family. Therefore, in this study, we identified 41 CIPK genes and 16 CBL genes in quinoa by bioinformatics, and studied their phylogeny, gene structure, conserved motifs, promoter elements and expression profile. Furthermore, we investigated the expression patterns of CIPK-CBL members in roots and leaves under drought stress. Our findings will provide valuable references for the further utilization of CBL-CIPK genes for the development of drought-tolerant plants in the context of global land loss, and will facilitate the functional characterization of individual CBLs and CIPKs gene responses to stress and developmental signals.

Identification of quinoa CIPK-CBL gene family
In the end, we identified 41 CIPK and 16 CBL members in quinoa and named them CqCIPK01-CqCIPK41 and CqCBL01-CqCBL16 (Table S2). The analysis of physical and chemical properties showed that the number of amino acids of CqCIPK protein is between 276 aa (CqCIPK07) and 613 aa (CqCIPK25), and the molecular weight is 30,943.37 Da (CqCIPK07)-68,335.48 Da (CqCIPK25), which is basically synchronized with the changing trend of the number of amino acids. The isoelectric point is between 5.29 (CqCIPK07) and 9.83 (CqCIPK25). In addition, the instability coefficient is between 30.01 (CqCIPK38) and 47.06 (CqCIPK04), most of which (80.49%) belong to stable proteins (proteins with an instability coefficient less than 40). The fat index is 78.56 (CqCIPK25)-100.53 (CqCIPK23). The amino acid number of CqCBL protein was between 135 (CqCBL15) and 381 (CqCBL10), and the instability coefficient was between 32.40 (CIPK07) and 50.75 (CqCIPK14). The hydrophobic coefficients of 57 CqCIPK-CBL proteins were all less than 0, which indicated that CqCIPK-CBL proteins were hydrophilic proteins. Subcellular localization prediction showed that 18 CqCIPK proteins and 2 CqCBL proteins were located in plasma membrane, 8 CqCIPK proteins and 7 CqCBL proteins were located in microbody, and 8 CqCIPK proteins were located in nucleus, 6 CqCIPK proteins and 7 CqCBL proteins were located in cytoplasm (Table S2).

Phylogenetic tree construction, gene structure and conservative motif analysis
The CIPK-CBL amino acid sequences of quinoa, pepper, rice and Arabidopsis (Table S3) were compared and phylogenetic trees were constructed by neighbor-joining method. According to the similarity of sequences, CBL proteins were divided into five subfamilies (Fig. 1A), namely, A, B, C, D and E, each subgroup contains a different percentage of its gene members, and the CIPK proteins of different species were grouped into six subfamilies (Fig. 1B), namely, A, B, C, D, E and F. For the CIPK family, F subfamily has the most CqCIPK members (14), and B and D subfamily have the least CqCIPK members (2). In addition, 20 pairs of paralogous gene were found in quinoa CqCIPK (except CqCIPK30), 7 pairs of paralogous gene were found in Arabidopsis AtCIPK and 6 pairs of paralogous gene were found in capsicum CaCIPK. For the CBL family, 7, 2, 2 and 1 pairs of paralogous gene were found in quinoa, Arabidopsis, rice and pepper respectively. There are no orthologous gene pairs between different species, which indicates that the CIPK and CBL genes are highly conserved during the evolution.
The structural analysis of CqCIPK genes showed that the family genes were divided into two types ( Fig. 2A): intron-enriched and intron-deleted. The number of exons in A, B, C, D and E is between 1 and 4 and the whole sequence of most genes is exon, such as CIPK07, CIPK09, CIPK15 and CIPK33 in group A, and CIPK20 in group B, CIPK02, CIPK06, CIPK16, CIPK18, CIPK27, CIPK34 and CIPK41 in group C, CIPK01, CIPK08, CIPK35 and CIPK37 in group E all had only one exon, and all of them had deletion of intron, we think it might have the same function. In contrast, the number of introns in subfamily F ranges from 11 to 15, in addition, most genes have non-coding regions at the 5'and 3'ends. Compared with other subgroups, Subgroup F has more introns and belongs to the intron enrichment class, but the distribution positions on exons are different and the length of sequences are also different. The CqCBL subfamilies also different greatly in gene structure (Fig. 2B). The exons of CqCBL were 5-13, and some genes did not have the non-coding region (CqCBL05, CqCBL11, CqCBL12, CqCBL14-CBL16).
In addition, we found 10 conservative motifs in the CqCIPK-CBL family. It was found that the motif number of CqCIPK proteins was between 6 and 10 ( Fig. 3A). The CqCIPK protein (except CqCIPK41) in group B, C and E all had 10 conservative motifs. 7 CqCIPK proteins in group A had motif numbers between 6 and 9. The motif numbers of 2 CqCIPK proteins in group D were 9. The motif numbers of 14 CqCIPK proteins in group F ranged from 7 to 10. The motif number of CqCBL proteins was 3-7 ( Fig. 3B), in which motif 1, motif 6 and motif 7 were found in all CqCBL genes, indicating that these three motifs were highly conserved in 16 CqCBL genes. In addition, we found that the number and location of motifs in different subfamilies are basically the same, and they are highly conservative. We assumed that their domains and functional units are basically similar within the same subfamily.

Analysis of go enrichment, protein interaction and cis-acting regulatory element
The Gene Ontology database was used to analyze the intracellular roles of CqCIPK and CqCBL proteins to comprehensively characterize the properties of CqCIPK and CqCBL genes and gene products. The results showed that CqCIPK-CBL proteins were involved in different functions ( Fig. 4A- and binding to ions (GO: 0043167). Interestingly, 41 CIPK proteins have protein kinase activity; 15 CBL proteins have calcium ion binding activity (GO: 0005509). In the aspect of biological process (BP), CqCIPK proteins are mainly involved in anatomical structure development, cellular protein process, signal transduction, and CqCBL proteins are mainly involved in nine biological processes.
Genes usually carry out their biological functions and signal transduction pathways through interacting networks. Investigation of the potential interaction networks associated with gene families can lead to a better understanding of their function. Studies have shown that CIPK mediates multiple biological processes through its interaction with CBL. Therefore, a possible interaction network of quinoa CIPK-CBL needs to be identified in order to better understand their biological functions. Based on the CIPK-CBL homologous genes of Arabidopsis thaliana, the CIPK-CBL protein interaction network of quinoa was constructed by STRING software, and 20 interacting Arabidopsis thaliana proteins with high confidence were identified, 41 CIPK proteins and 16 CBL proteins also appear in the known protein-protein network diagram in quinoa (Fig. 5). These proteins that interact with CIPK proteins include calcium-binding CBLS (CBL2, SIP3, SIP4 and CBL10), AKTs associated with potassium transport, and SOSs associated with hydrogen transport. Previous functional analyses have demonstrated that these interactions are involved in plant ion regulation, developmental processes and hormone signal transduction and abiotic stress responses [1,31].
Cis-acting regulatory element is a specific motif existing in the promoter region of a gene, which can combine with transcription factors to regulate the downstream genes [32]. Therefore, the identification and analysis of cis-acting regulatory elements in gene promoter regions is helpful to further enhance our understanding of the molecular regulation of these genes. In this study, we analyzed 2000 bp upstream sequences of 41 CqCIPK genes and 16 CBL genes, and found 23 types of cisacting elements (Fig. 6, Table S4), involving hormone, pressure and tissue-specific expression. Abscisic acid (ABA)-responsive element (ABRE), CGTCA-motif and TGACG-motif (methyl jasmonate response element) were found in the promoter region of most of the CIPK and CqCBL genes. In stress response, TC-rich repeats responded to various defense responses, and existed in single copy in the promoter regions of 7 CIPK genes and 3 CBL genes. LTR (low-temperature responsiveness) element was found in the promoter region of 16 CqCIPK genes and 4 CqCBL genes in response to low temperature. MBS (MYB binding site) element involved drought induction and could be found in the promoter region of 21 CqCIPK genes and 11 CqCBL genes. The promoter region of CqCBL14 gene contained 6 MBS elements. In   The putative cis-regulatory element and transcription factor binding sites in the promoter region of CBL and CIPK genes of quinoa. The colors and numbers on the grid indicate the number of different cis-regulatory element in the CBL and CIPK genes the regulation of flavonoid biosynthesis genes. In addition, RY-element (involved in seed-specific regulation) only exists in CqCIPK10, NON-box in CqCIPK26 and CqCIPK30. These results indicated that CqCIPK and CqCBL genes were involved in the growth and stress response of quinoa.

Expression pattern analysis of CqCIPK-CBL gene in different tissues and treatments
At the same time, we analyzed the expression patterns of CIPK-CBL family members in roots and shoot apices under different abiotic stresses ( Fig. 7A-B, Table  S5) using transcriptome data. We found that CqCBL05, CqCBL09, CqCIPK06, CqCIPK12, CqCIPK32 and CqCIPK41 genes were not expressed in control and in all treatments (salt, drought, high temperature and low phosphorus). In addition, we found that most of the genes (CqCBL04, CqCBL06, CqCBL08, CqCBL10, CqCBL11, CqCBL13, CqCIPK03-CqCIPK05, CqCIPK07, CqCIPK10, CqCIPK14, CqCIPK15, CqCIPK21, CqCIPK24, CqCIPK25, CqCIPK35, CqCIPK36 and CIPK38) expressed less in salt, drought and high temperature than control, some genes (CqCBL02, CqCBL03 and CqCBL07; CqCIPK01, CqCIPK02, CqCIPK08, CqCIPK16, CqCIPK18 and CqCIPK37) were significantly increased under drought stress compared with control, these results suggested that these genes may be involved in drought stress and play a positive regulatory role. The expression of four genes (CqCBL06, CqCBL10, CqCIPK05 and CqCIPK38) in shoot apex under low phosphorus, drought and salt stress was significantly lower than that in control, drought stress and salt stress play a negative role in regulation. The expression of CqCIPK02 gene in root and shoot tip was significantly higher than that in control. CqCIPK02 gene may play a positive role in phosphorus deficiency. The expression of some genes in root and shoot tip (CqCBL03, CqCBL07, CqCIPK08, CqCIPK16, CqCIPK18, CqCIPK34, CqCIPK36, CqCIPK37 and CqCIPK39) was significantly higher than that of control under drought stress. These results suggested that CqCIPK-CBL family genes are involved in various abiotic stresses in different ways at the transcriptional level.
Studies have shown that CIPK-CBL family genes are involved in different stages of development. Therefore, we studied the expression patterns of the family genes in different tissues and organs by using transcriptome data ( Fig. 8A-B). The results showed that most CIPK genes were expressed in all tissues and organs. Among them, CqCBL05, CqCBL09, CqCIPK01, CqCIPK06, CqCIPK09, CqCIPK11, CqCIPK35 and CqCIPK41 were almost not expressed in many tissues and organs. CqCBL03, CqCBL13, CqCIPK05, CqCIPK16 and CqCIPK38 were highly expressed in all tissues and treatments, especially in internode stems, seedling flowers, flowers of white sweet quinoa, inflows and leaves. CqCBL15, CqCIPK04, CqCIPK20 and CqCIPK31 had relatively low expression abundance in all tissues and treatments. Some genes have tissue specificity (CqCBL01, CqCBL08, CqCBL12, CqCIPK07, CqCIPK12, CqCIPK15, CqCIPK26 and CqCIPK30). For example, CqCBL01 was highly expressed in seedling and almost not expressed in fruit of yellow bitter quinoa, CqCIPK07 was highly expressed in internode stems, seedling and inflows, but almost not expressed in leaves petioles and dry seeds, and CqCIPK12 was almost not expressed in fruit of white sweet quinoa, the CqCIPK15 gene was overexpressed in seedling, inrescuences and flowers of white sweet quinoa, but not expressed in leaves petioles and dry seeds. The CqCIPK26 gene was overexpressed in internode stems and leaves, but not in fruit of white sweet quinoa and fruit of yellow bitter quinoa. CqCIPK30 gene was overexpressed in internode stems but not in fruit of white sweet quinoa. In addition, we can observe that the expression patterns of most genes that belong to the lineal homologue are consistent (CqCBL11/CBL15, CqCIPK07/CIPK15, CqCIPK17/CIPK33, CqCIPK09/CIPK11).

RT-qPCR validated the expression pattern of CqCIPK-CBL genes in leaves and roots of quinoa under drought stress
In addition, RT-qPCR was used to detect the expression pattern of CqCIPK-CBL members in quinoa roots under drought stress (Fig. 9). In the roots, all the members responded to drought stress at different time points after drought treatment, and there were significant differences compared with the control, 10 genes (CqCBL04, CqCBL07, CqCIPK01, CqCIPK06, CqCIPK07, CqCIPK09, CqCIPK12, CqCIPK15, CqCIPK32 and CqCIPK37) were extremely sensitive to drought stress in roots. The relative expression of these 10 genes was at least 40 times that of the control at some point after drought stress, the relative expression of CqCBL04, CqCIPK15 and CqCIPK37 were 145 times, 242.10 times and 162.53 times, respectively.
In leaves (Fig. 10), the relative expression of a few genes (CqCBL09, CqCBL14, CqCIPK05, CqCIPK24, CqCIPK29, CqCIPK32 and CqCIPK38) was significantly lower than that of control after drought stress, which indicated that these genes played a negative role in drought stress. At the same time, most of the genes showed two expression patterns under continuous drought stress: The first pattern: the relative expression of 27 genes increased with the increase of drought degree, and reached the maximum 9 h after drought stress. The relative expression of CqCBL13, CqCIPK11 and CqCIPK37 were 157 times, 115.76 times and 160.79 times, respectively. In the second model, the relative expression of 13 CqCIPK genes increased at first and then decreased with the increase of drought stress, and all of them reached the maximum at 6 h after drought stress. The relative expression of CqCIPK01 and CqCIPK25 on the 6 h were 77.06 and 138.53 times, respectively. The relative expression of  6 CqCBL genes were (CqCBL01-CqCBL02, CqCBL04, CqCBL09-CqCBL10 and CqCBL14) decreased first and then increased, and all of them reached the maximum on the 9 h. In addition, we observed an interesting phenomenon, the expression of most CqCIPK genes and CqCBL genes increased sharply in 3-6 h after drought stress (CqCBL07, CqCBL11, CqCIPK01, CqCIPK02, CqCIPK04, CqCIPK25, and CqCIPK27), the results indicated that these genes strongly responded to drought stress in the 3-6 h after drought stress.

Subcellular localization of CqCIPK14 gene and detection of yeast self-activation
In order to study the function of CqCIPK14, we studied its subcellular localization. CqCIPK14 was fused with GFP under the 35S promoter and expressed instantaneously in Nicotiana tabacum L. The results showed that CqCIPK14-GFP was localized in the nucleus of Nicotiana tabacum L. (Fig. 11A). In addition, we performed a transcriptional activation test to study the self-activation activity of CqCIPK14 (Fig. 11B). PGBKT7-53 × PGADT7-T (positive control), PGBKT7-LAM × PGADT7-T (negative control) and PGBKT7-CIPK14 × PGADT7(experimental group) all grew on SD/−Trp-Leu medium, which indicated that the plasmids were transformed successfully. CqCIPK014 no grow and turn blue on SD/Trp-Leu-His + x-α-gal medium and SD/Trp-Leu-His-Ade + x-α-gal medium. It is proved that there is no self-activation in CqCIPK14, which can be used in follow-up study.

Discussion
CIPK-CBL family genes are involved in the regulation of plant responses to biotic and abiotic stresses, and play an important role in many plant life activities [33]. In recent years, the CBL-CIPK pathway in model plants has been studied with great success, but the precise function and mechanism of the CIPK-CBL family genes are still unclear, the study of the CIPK-CBL family genes in quinoa could provide a theoretical basis for further investigation of the interaction between CBL and CIPK proteins in quinoa, and improve the stress resistance of quinoa in molecular breeding and transgenic breeding. Therefore, the whole genome of the CIPK-CBL gene family in quinoa was identified by the bioinformatics method, and 41 CIPK and 16 CBL members were screened by sequence alignment method, which were similar to 43 CIPK genes in maize [34]. The CIPK-CBL gene has been found in many plants: 10 AtCBL and 26 AtCIPK genes [9] in Arabidopsis, there were 10 OsCBL and 33 OsCIPK genes in rice [10], 8 VvCBL and 20 VvCIPK genes in grape [12], 9 CaCBL and 26 CaCIPK genes in pepper [15], 23MsCBL and 58 MsCIPK genes in Alfalfa [17]. Studies have shown that these variations in the number of CBL-CIPK genes between different species are due to events of gene duplication and loss during evolution [35], and that there are multiple CBL-CIPK genes in the quinoa genome, indicating functional diversity of the CBL-CIPK family. In addition, 40 CIPK genes (except CqCIPK30) formed 20 pairs of homologous genes, which indicated that most CqCIPK genes were extended in a species-specific manner during the long evolution of plants, this phenomenon has also been extensively demonstrated in the study of other gene families in plants [36]. Intron-exon gene structure is a typical mark of evolution of some gene families [37]. In this study, we found that the gene structure of different subfamily has some similarity. According to the number of introns, 41 CqCIPK genes were classified into two types, intron-enriched type (with nine or more introns) and intron-poor type (without or with only one intron), the intron-deficient gene system occurs after the intronenriched gene, which may occur when the intronenriched gene is reinserted into the genome during the reverse transcription process [38]. So far, the same results have been found in maize, poplar, suggesting that the CIPK gene sequence is structurally conserved [10]. The intron loss is faster than the intron gain during gene segment replication, so the intron-enriched CqCIPK may have higher similarity to the original gene. Less intron CqCIPK genes were enriched in group A-E, and more intron genes were clustered in group F, which indicated that the genes of the intron enriched group were closely related to each other, and the genes of the intron deleted group were closely related to each other, this condition is also reported in the cassava MeCIPK genes [33], which may be due to gene duplication. These data suggested that intron acquisition and loss events play an important role in the evolution of the CIPK family. It was found that one CqCBL protein could interact with one or more CqCIPK proteins. Similarly, a single CqCIPK protein can interact with one or more CqCBL proteins, consistent with findings in cassava and pepper [33].
Cis-acting regulatory elements, as key molecular switches, are involved in regulating the transcriptional regulation of gene activity in various biological processes [14]. The analysis of promoter region of CqCIPK-CBL genes showed that CqCIPK-CBL genes contained cis-regulatory elements related to environmental stress and hormone induction, which may endow the genes with the potential function of responding to stress and regulating endogenous hormones. When plants are subjected to external stress, such as drought, high temperature, salt and other stress, these stress signals are transformed into signal factors through a series of signals, activating the corresponding transcription factors, and binds to the cis-regulatory element of the corresponding gene, thus activating the expression of the relevant genes in response to external adversity signals [39]. In this study, 10 hormone response elements were found in the promoter region of the CIPK-CBL genes in quinoa. ABRE elements were found in the upstream of 36 CIPK-CBL genes. The ABRE elements were also found in Arabidopsis, rice and honeysuckle [9,10,14], it is suggested that CIPK-CBL genes are involved in the ABA signaling pathway, which is mainly involved in stomatal closure, cold, drought and salt stress [14]. In addition, the MBS elements (drought response element) were found in the upstream of 32 CIPK-CBL genes, which was mainly involved in drought-induced response [16]. Therefore, these genes may play a key role in enhancing the resistance of quinoa. The CIPK-CBL family genes are involved in many stages of plant growth and development [40]. Therefore, the expression patterns of CIPK-CBL family genes in many tissues of quinoa were analyzed by transcriptome data-to better understand their role in plant growth and development. The results showed that 35 CqCIPK and 16 CBL genes were expressed in all the test organs, and the majority of CqCIPK-CBL genes expressed differently in different germplasms of special tissues, which may contribute to the functional diversity of different germplasms of special tissues. In addition, AtCIPK19 was detected in pollen grains and pollen tubes, especially at much higher levels than in other tissues, and there were differences in tube growth and polarity between AtCIPK19 overexpression, mutants and complementary lines, indicates that these processes require AtCIPK19 [41]. In this study, CqCIPK05, CqCIPK16 and CqCIPK38 were also highly expressed in pollen and inflorescence. The flowering time gene, Gigantea (GI), plays a major role in the control of photoperiod and circadian rhythm. AtCIPK24 is captured by GI rather than SOS1 under normal conditions, but the complex is degraded in the presence of salt, this provides a unique mechanism between plant  [42]. SlCIPK2 was specifically detected in tomato flower organs and interacted with several SlCBL genes and some stress response transcription factors, indicating that SlCIPK2 participates in stamen development and stress tolerance through calcium signal transduction [43]. In this study, CqCBL03, CqCBL13, CqCIPK02, CqCIPK07 and CqCIPK16 genes were highly expressed in flower organs of different quinoa cultivars. CqCBL03, CqCBL06, CqCIPK02, CqCIPK16, CqCIPK38 and CqCIPK39 were highly expressed in stem and leaf. This is consistent with CIPK-CBL in M.domestica and O. sativa [11,44]. CqCBL03, CqCBL06, CqCBL07, CqCBL13, CqCIPK02, CIPK05, CIPK10 and CIPK13 were highly expressed in apical meristems. CqCBL03, CqCBL07, CqCIPK02, CIPK05 and CIPK16 were highly expressed in fruits, indicating that they might affect seed size and embryo development, this is consistent with the previous results in Arabidopsis and Prunus mume [45,46]. These results suggested that CqCIPK-CBL genes may play an important role in the growth and development of quinoa.
In conclusion, the expression profiles of CIPK-CBL genes in different tissues will provide clues for the further study on the development of quinoa.
The CIPK-CBL genes have been shown to play an important role in plant stress, especially in response to drought stress [47]. For example, 4 AtCIPKs (AtCIPK6,  [48]. In Arabidopsis, it is found that AtCIPK16 has a positive regulatory effect on plant salt tolerance, and AtCIPK23 has a negative regulatory effect on plant drought resistance [49,50]. AtCIPK7 regulates cold stress response through interaction with AtCBL1 [19]. MtCBL7 was upregulated by PEG, NaCl and ABA stress in Alfalfa [48]. Zhao [51] found that ZmCIPK16 can respond to drought, high salt and ABA induction in a maize study. Piao [52] found that the rice mutant OsCIPK31 was highly sensitive to drought and high salt stress during seedling growth and seed germination. A small number of genes in this study (CqCIPK05, CqCIPK24, CqCIPK29, CqCIPK32 and CqCIPK32) play a negative regulatory role in leaf drought stress, and similar situations have also occurred in soybeans [53]. Overexpression of OsCIPK23 in rice can increase the expression level of droughtrelated genes to improve rice drought tolerance [52]. In this study, the expression of 57 CqCIPK-CBL genes in roots was significantly increased under drought stress, and strongly responded to drought stress, indicating that this family of genes may be involved in drought tolerance in roots, which is consistent with the study in pigeon pea [22]. In addition, previous studies have found that CcCIPK14-CcCBL1 in pigeon pea positively regulates drought tolerance by enhancing the biosynthesis of flavonoids [22], and the absorption of potassium ions by the AtCBL1/9-AtCIPK23-AKT1 signaling pathway in Arabidopsis leads to the effects of potassium ions on plant leaves. The stomata are closed, which strengthens the ability of the leaves of the plant to lock water, and indirectly improves the drought resistance of the plant [54]. Down-regulating the expression of OsCIPK23 gene in rice reduces the resistance of rice to drought stress [29]. The heterologous expression of TaCIPK2, TaCIPK23 and TaCIPK27 in wheat enhances the drought resistance of transgenic Arabidopsis plants through an abscisic aciddependent pathway [25]. Overexpression of the apple MdCIPK6L gene in tomato improves the drought resistance of the plant [55]. In this study, 41 CqCIPK genes directly or indirectly interacted with 16 CqCBL genes, indicating that the responses of these genes to drought stress were also mediated by the CBL-CIPK pathway. The above results suggested that CBL-CIPK can enhance drought tolerance by regulating K + and ABA signaling pathways, which provides a good direction for breeding high-yielding and drought-tolerant crop varieties, it also indicates that there are many drought tolerance regulation mechanisms in different crops.

Conclusions
In this study, we identified 16 CBL and 41 CIPK genes in quinoa. The functions of these 2 family genes were characterized according to phylogenetic tree, gene structure, conserved sequence, cis-acting regulatory element, GO enrichment and drought stress. It was found that CqCIPK-CBL genes strongly responded to drought stress in roots and leaves. In addition, we further studied subcellular localization and detection of yeast selfactivation of CqCIPK14 gene, and the results showed that CqCIPK14-GFP was localized in the nucleus of Nicotiana tabacum L and there is no self-activation in CqCIPK14. Therefore, the results of this study provided a solid foundation for further functional research of CBL-CIPK network.

Identification of quinoa CIPK-CBL family genes
Quinoa genome data and structural annotation information were downloaded from the Phytozome 12 database (https:// phyto zome. jgi. doe. gov/ pz/ portal. html). The Arabidopsis, rice, and pepper of CIPK-CBL gene sequences were downloaded from the Plant TAIR database (https:// www. arabi dopsis. org/) and Ensembl Plants database (http:// plants. ensem bl. org/). Using Arabidopsis CIPK and CBL gene family members as probes to pre-screen the quinoa CIPK and CBL protein, the E-value value is less than 0.01; Pre-screened biomolecular structure were submitted to the NCBI-swisprot database (http:// plants. ensem bl. org/) for homology comparison, remove the close-source sequence of quinoa CIPKs, and keep the non-redundant protein sequence. The obtained quinoa CIPK and CBL protein sequence were submitted to Expasy (https:// web. expasy. org/ compu te_ pi/) to predict their basic physics and chemical property, such as amino acid numbers, isoelectric point and hydrophobicity. The subcellular location was predicted through WoLF PSORT (http:// www. gensc ript. com/ wolf-psort. html).

Construction of phylogenetic tree, analysis of gene structure and conserved motif of quinoa CIPK-CBL family
Use the MEGA 7 tool to perform sequence alignment on the CIPK and CBL protein sequences of quinoa, Arabidopsis, rice and pepper. Based on the results of multiple sequence alignments, Neighbor-joining (NJ) was used to construct a phylogenetic tree; parameter settings: method was poisson model, the number of bootstrap test was adjusted to 1000, and missing data treatment was adjusted to pairwise deletion.
The GFF annotation information of CqCIPK and CBL genes were submitted to the gene structure display server 2.0(GSDS 2.0, http:// gsds. cbi. pku. edu. cn/) for Genetic Structure Analysis. In addition, the amino acid sequences of CqCIPK and CBL proteins were submitted to Multiple Em for Motif Elicitation (MEME, http:// meme-suite. org/ tools/ meme) for analysis of conservative motifs, parameter setting: site distribution is any number of times, conservative the upper limit of the motif is 10, the size of the motif is 10 ~ 60 bp, and other parameters are defaulted.

GO enrichment, protein interaction network and cis-regulatory element in the promoter region
The CqCIPK-CBL protein sequences were submitted to the blast2go software (https:// www. blast 2go. com/), and use NCBI-blast as the comparison database to perform GO (gene ontology) functional analysis of the CqCIPK-CBL family genes [56]. Based on the Arabidopsis CIPK homologous genes, software String 10 (http:// string-db. org/) was used to predict the protein interaction network map.

Plant material and treatments
The experiment was conducted in the Plant Physiology Laboratory of the College of Life Science and Technology, Gansu Agricultural University of China from March 2021 to July 2021. The test material was potted seedlings of 'Long Li No. 2'(from Gansu Academy of Agricultural Sciences). On March 3, 2021, seeds with full grains were selected and sterilized with 5% NaClO for 15 minutes, rinsed with water three times, and thirty seeds were sown in a flower pot with a diameter of 30 cm (Volumen =9.2 L). Mix the turf soil and vermiculite (mixing ratio is 3:1) as a cultivation soil. The culture conditions were: light at 25 °C for 16 h, darkness at 20 °C for 8 h, relative humidity 70-75%, light intensity 450 μmol·m − 2 ·s − 1 . When the seedlings grow to the 4-leaf stage, robust, consistent and non-polluting seedlings were selected for drought treatment: 20% PEG. The leaves and roots of quinoa seedlings were taken 0 h, 3 h, 6 h and 9 h after treatment. Three biological replicates for each treatment. The leaves and roots were frozen quickly with liquid nitrogen and were placed at − 80 °C for later use.

Expression pattern analysis, RNA extraction, cDNA synthesis and quantitative PCR
The transcriptome data of different tissues and organs of quinoa (No: PRJNA394651) and different treatments (No: PRJNA306026) were obtained from Bioproject database (www. ncbi. nlm. nih. gov/ biopr oject). RNA extraction was performed using the plant extraction kit RNAplant-RTR2303 (Zhong ke rui tai Biotechnology Co., Ltd., Beijing) and proceeded according to the operating instructions. Use Agilent 2100 Bioanalyzer and Nan-oDrop to test the integrity and purity of RNA respectively. After passing the test, RNA was placed at − 80 °C for later use. Primer ScriptTM RT Regent Kit with gDNA Eeaser (TaKaRa, Shanghai) kit was used for reverse transcription to obtain cDNA, and SYBR Primer Ex TaqTM II (TaKaRa) kit was used for quantification. Quantitative PCR instrument is Light Cycler ® 96 Real-Time PCR System (Roche, Switzerland). TUB-9 was taken as an internal reference gene, 57 genes were quantified for RT-qPCR (41 for CIPK and 16CBL), the primer information for 58 genes was listed in Table S1. The reaction system is 20 μL: 1 μL cDNA, 1 μL of the upstream and downstream primers, 10 μL of SYBR, and 7 μL of ddH 2 O. The reaction program is: 95 °C pre-denaturation for 30 s, 95 °C denaturation for 10 s, and 60 °C annealing for 30 s, 72 °C extension 30 s, 40 cycles, repeat 3 times. After the reaction, the fluorescence value change curve and melting curve are analyzed. The relative expression of genes was calculated using 2 -ΔΔCT [58].